Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
Duchenne muscular dystrophy (DMD) is an X-linked recessive genetic disorder for which the biochemical defect is as yet unknown. Recently, two cloned segments of human X-chromosome DNA have been described which detect structural alterations within or near the genetic locus responsible for the disorde...
Váldodahkkit: | Kunkel, L, Hejtmancik, J, Caskey, C, Speer, A, Monaco, A, Middlesworth, W, Colletti, C, Bertelson, C, Müller, U, Bresnan, M, Shapiro, F, Tantravahi, U, Speer, J, Latt, SA, Bartlett, R, Pericak-Vance, M, Roses, A, Thompson, M, Ray, P, Worton, R, Fischbeck, K, Gallano, P, Coulon, M, Duros, C, Boue, J |
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Materiálatiipa: | Journal article |
Giella: | English |
Almmustuhtton: |
1986
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Geahča maid
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Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
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Almmustuhtton: (1985) -
Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families.
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Almmustuhtton: (1986) -
Molecular genetics of Duchenne muscular dystrophy.
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Almmustuhtton: (1986) -
Recombination with pERT87 (DXS164) in families with X-linked muscular dystrophy.
Dahkki: Fischbeck, K, et al.
Almmustuhtton: (1986) -
Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
Dahkki: Monaco, A, et al.
Almmustuhtton: (1987)